A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4880



Internal ID15542991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177971688..177986678hg38UCSC Ensembl
Outerchr5:177398689..177413679hg19UCSC Ensembl
Outerchr5:177331295..177346285hg18UCSC Ensembl
Outerchr5:177331295..177346285hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387539
hg197539
hg187539
hg177539
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5152
Supporting Variants
SamplesNA19129
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4880
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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